Congenital alacrima in a patient with G (Opitz Frias) syndrome |
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| Authors: | Munis Dundar Kuddusi Erkiliç Fatma Demiryilmaz Mustafa Küçükaydin Mustafa Kendirci Hamit Okur Ahmet Kazez |
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| Institution: | (1) Department of Medical Genetics, School of Medicine, Erciyes University, TR-38039 Kayseri, Turkey, TR;(2) Department of Ophthalmology, School of Medicine, Erciyes University, TR-38039 Kayseri, Turkey, TR;(3) Department of Pediatric Surgery, School of Medicine, Erciyes University, TR-38039 Kayseri, Turkey, TR;(4) Department of Pediatrics, School of Medicine, Erciyes University, TR-38039 Kayseri, Turkey, TR |
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| Abstract: | Congenital alacrima is an autosomal dominant disorder showing markedly deficient lacrimation and punctate corneal epithelial
erosions. The G (Opitz-Frias) syndrome is also an autosomal dominant disorder characterised by hypertelorism, hypospadias,
stridor, and dysphagia. Here we report a 5-year-old boy with the G syndrome presenting congenital alacrima.
Received: 23 August 1995 / Revised: 25 September 1995 |
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